Raimundo S - Search Results

1

Elucidation of the genetic basis of the common 'intermediate metabolizer' phenotype for drug oxidation by CYP2D6.

Raimundo S, Fischer J, Eichelbaum M, Griese EU, Schwab M, Zanger UM. Raimundo S, et al. Pharmacogenetics. 2000 Oct;10(7):577-81. doi: 10.1097/00008571-200010000-00001. Pharmacogenetics. 2000. PMID: 11037799

2

Cytochrome P450 2D6: overview and update on pharmacology, genetics, biochemistry.

Zanger UM, Raimundo S, Eichelbaum M. Zanger UM, et al. Among authors: raimundo s. Naunyn Schmiedebergs Arch Pharmacol. 2004 Jan;369(1):23-37. doi: 10.1007/s00210-003-0832-2. Epub 2003 Nov 15. Naunyn Schmiedebergs Arch Pharmacol. 2004. PMID: 14618296 Review.

3

A novel intronic mutation, 2988G>A, with high predictivity for impaired function of cytochrome P450 2D6 in white subjects.

Raimundo S, Toscano C, Klein K, Fischer J, Griese EU, Eichelbaum M, Schwab M, Zanger UM. Raimundo S, et al. Clin Pharmacol Ther. 2004 Aug;76(2):128-38. doi: 10.1016/j.clpt.2004.04.009. Clin Pharmacol Ther. 2004. PMID: 15289790

4

Impaired expression of CYP2D6 in intermediate metabolizers carrying the *41 allele caused by the intronic SNP 2988G>A: evidence for modulation of splicing events.

Toscano C, Klein K, Blievernicht J, Schaeffeler E, Saussele T, Raimundo S, Eichelbaum M, Schwab M, Zanger UM. Toscano C, et al. Among authors: raimundo s. Pharmacogenet Genomics. 2006 Oct;16(10):755-66. doi: 10.1097/01.fpc.0000230112.96086.e0. Pharmacogenet Genomics. 2006. PMID: 17001295

5

A silent mutation (2939G>A, exon 6; CYP2D6*59) leading to impaired expression and function of CYP2D6.

Toscano C, Raimundo S, Klein K, Eichelbaum M, Schwab M, Zanger UM. Toscano C, et al. Among authors: raimundo s. Pharmacogenet Genomics. 2006 Oct;16(10):767-70. doi: 10.1097/01.fpc.0000236331.03681.24. Pharmacogenet Genomics. 2006. PMID: 17001296

6

Comprehensive analysis of the genetic factors determining expression and function of hepatic CYP2D6.

Zanger UM, Fischer J, Raimundo S, Stüven T, Evert BO, Schwab M, Eichelbaum M. Zanger UM, et al. Among authors: raimundo s. Pharmacogenetics. 2001 Oct;11(7):573-85. doi: 10.1097/00008571-200110000-00004. Pharmacogenetics. 2001. PMID: 11668217

7

A natural variant of the heme-binding signature (R441C) resulting in complete loss of function of CYP2D6.

Klein K, Tatzel S, Raimundo S, Saussele T, Hustert E, Pleiss J, Eichelbaum M, Zanger UM. Klein K, et al. Among authors: raimundo s. Drug Metab Dispos. 2007 Aug;35(8):1247-50. doi: 10.1124/dmd.107.015149. Epub 2007 Apr 25. Drug Metab Dispos. 2007. PMID: 17460029

8

Cloning and sequence of partial cDNAs encoding the human type V and VI adenylyl cyclases and subsequent RNA-quantification in various tissues.

Raimundo S, Giray J, Volff JN, Schwab M, Altenbuchner J, Ratge D, Wisser H. Raimundo S, et al. Clin Chim Acta. 1999 Jul;285(1-2):155-61. doi: 10.1016/s0009-8981(99)00067-4. Clin Chim Acta. 1999. PMID: 10481931

9

[Solitary pulmonary nodule as an unusual presentation of infection by Mycobacterium abscessus. Report of a clinical case].

Gutiérrez J, Yumay P, Schiappacasse G, Raimundo S, Valenzuela H, Cabello H. Gutiérrez J, et al. Among authors: raimundo s. Rev Med Chil. 2023 Dec;151(12):1636-1639. doi: 10.4067/s0034-98872023001201636. Rev Med Chil. 2023. PMID: 39270086 Free article. Spanish.

10

Hypertrophic Osteoarthropathy: A Case of an Undifferentiated Polyarthritis.

Carvalho MM, Raimundo S. Carvalho MM, et al. Among authors: raimundo s. Cureus. 2023 Dec 27;15(12):e51145. doi: 10.7759/cureus.51145. eCollection 2023 Dec. Cureus. 2023. PMID: 38283429 Free PMC article.

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